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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309038copy number variation2nstd102humanUncertain significance GRCh37 chr11: 128,781,169-128,786,626 , GRCh38.p12 chr11: 128,911,274-128,916,731 KCNJ5
    nsv4457039copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,786,032-128,890,846 , GRCh38.p12 chr11: 128,916,137-129,020,951 KCNJ5, TP53AIP1, 2 more genes
    nsv3911009copy number variation1nstd102humanPathogenic GRCh38 chr11: 119,424,297-135,075,271 , NCBI36 chr11: 118,800,217-134,450,377 , GRCh37 chr11: 119,295,007-134,945,165 KCNJ5, PHB1P17, 304 more genes
    nsv3922773copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617 KCNJ5, ETS1-AS1, 301 more genes
    nsv3906843copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,538,664-134,938,470 , GRCh38.p12 chr11: 119,667,954-135,068,576 KCNJ5, TMEM225, 296 more genes
    nsv3902675copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,807,473-134,868,407 , GRCh38.p12 chr11: 119,936,764-134,998,513 KCNJ5, FEZ1, 291 more genes
    nsv3923251copy number variation1nstd102humanPathogenic NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165 KCNJ5, KIRREL3-AS3, 279 more genes
    nsv3901752copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,527,021-134,938,470 , GRCh38.p12 chr11: 120,656,312-135,068,576 KCNJ5, LOC105369534, 276 more genes
    nsv4436748copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169 KCNJ5, LINC02098, 276 more genes
    nsv3904760copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,615,374-134,868,407 , GRCh38.p12 chr11: 120,744,665-134,998,513 KCNJ5, OR8D2, 275 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 KCNJ5, MIR8052, 275 more genes
    nsv3924566copy number variation1nstd102humanPathogenic GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160 KCNJ5, CCDC15-DT, 271 more genes
    nsv3891701copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,136,603-134,938,470 , GRCh38.p12 chr11: 121,265,894-135,068,576 KCNJ5, OR10G9, 266 more genes
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 KCNJ5, VSIG10L2, 268 more genes
    nsv3895234copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,416,261-134,938,470 , GRCh38.p12 chr11: 121,545,552-135,068,576 KCNJ5, SF3A3P2, 262 more genes
    nsv3918400copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,482,185-134,938,470 , GRCh38 chr11: 121,611,476-135,068,576 , NCBI36 chr11: 120,987,395-134,443,680 KCNJ5, RN7SL167P, 262 more genes
    nsv3915295copy number variation1nstd102humanPathogenic NCBI36 chr11: 121,064,970-134,450,377 , GRCh38 chr11: 121,689,052-135,075,271 , GRCh37 chr11: 121,559,760-134,945,165 KCNJ5, LOC105369591, 262 more genes
    nsv3892434copy number variation1nstd102humanPathogenic GRCh37 chr11: 121,501,072-134,868,348 , GRCh38.p12 chr11: 121,630,363-134,998,454 KCNJ5, ZNF123P, 261 more genes
    nsv3919969copy number variation1nstd102humanPathogenic GRCh38 chr11: 121,780,459-135,075,271 , GRCh37 chr11: 121,651,167-134,945,165 , NCBI36 chr11: 121,156,377-134,450,377 KCNJ5, STT3A-AS1, 262 more genes
    nsv3915055copy number variation1nstd102humanPathogenic NCBI36 chr11: 121,184,838-134,452,384 , GRCh37.p13 chr11: 121,679,628-134,946,516 , GRCh38.p12 chr11: 121,808,920-135,076,622 KCNJ5, KIRREL3, 262 more genes
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